Browse > Article
http://dx.doi.org/10.5352/JLS.2009.19.6.799

Evaluation of Radiation-induced Apoptosis in Seminiferous Tubule of ICR Mouse after Gamma Irradiation.  

Jang, Jong-Sik (Department of Animal Science, Kyungpook National University)
Kim, Joong-Sun (Animal Medical Center, College of Veterinary Medicine, Chonnam National University)
Kim, Jong-Choon (Animal Medical Center, College of Veterinary Medicine, Chonnam National University)
Kim, Sung-Ho (Animal Medical Center, College of Veterinary Medicine, Chonnam National University)
Publication Information
Journal of Life Science / v.19, no.6, 2009 , pp. 799-803 More about this Journal
Abstract
The killing of male germ cells by radiation and other toxicants has recently been attributed to apoptosis, but a critical evaluation of the presence of the different features of apoptosis in each epithelial stage has not been performed. In this study, mouse testes exposed to radiation were examined by light microscopy and terminal transferase-mediated end labeling (TUNEL) with periodic acid-Schiff (PAS) stains to determine whether the cells were apoptotic according to several criteria. Apoptosis was easily recognized by the presence of peroxidase-stained, entirely apoptotic bodies. In the TUNEL-positive cells or bodies, the stained products correlated precisely with the typical morphologic characteristics of apoptosis as seen at the light microscopic level. The changes that occurred from 0 to 24 hours after exposing the mice to 2 Gy of gamma-rays (2 Gy/min) were examined. The numbers of apoptotic cells reached a peak at 12 hours after irradiation and then declined. The mice that received 0-8 Gy of gamma-rays were examined 8 hours after irradiation. Dose-response relationships were generated for each stage of the epithelial cycle by counting TUNEL-positive cells. The dose-response curves were linear- quadratic [y=(-0.014${\pm}$0.009)$D^{2}$+(0.31${\pm}$0.697)D+0.3575. Where y=the number of apoptotic cells per seminiferous tubule, and D=the irradiation dose in Gy, $r^{2}$=0.9] and there was a significant relationship between the frequency of apoptotic cells and the radiation dose. Although the maximum response was produced by 8 Gy, even 0.5 Gy induced marked changes. These changes were most pronounced in B spermatogonia of stage V and the spermatocyte at the mitotic cells of stage XII.
Keywords
Gamma-ray; apoptosis; seminiferous tubule; epithelial stage;
Citations & Related Records
연도 인용수 순위
  • Reference
1 Oakberg, E. F. 1956. A description of spermiogenesis in the mouse and its use in analysis of the cycle of the seminiferous epithelium and germ cell renewal. Am. J. Anat. 99, 391-413   DOI   ScienceOn
2 Oakberg, E. F. 1955. Sensitivity and time of degeneration of spermatogenic cells irradiated in various stages of maturation in the mouse. Radiat. Res. 2, 369-391   DOI   ScienceOn
3 van der Meer, Y., R. Huiskamp, J. A. Davids, I. van der Tweel, and D. G. de Rooij. 1992. The sensitivity to X rays of mouse spermatogonia that are committed to differentiate and of differentiating spermatogonia. Radiat. Res. 130, 296-302   DOI   ScienceOn
4 Wyllie, A. H. 1981. Cell death: a new classification separating apoptosis from necrosis, pp. 9-34, In Bowen, I. D and R. A. Lockshin (eds.), Cell Death in Biology and Pathology, Chapman & Hall, London
5 Giampietri, C., S. Petrungaro, P. Coluccia, A. D'Alessio, D. Starace, A. Riccioli, F. Padula, F. Palombi, E. Ziparo, A. Filippini, and P. De Cesaris. 2005. Germ cell apoptosis control during spermatogenesis. Contraception 72, 298-302   DOI   ScienceOn
6 Hasegawa, M., G. Wilson, L. D. Russell, and M. L. Meistrich. 1997. Radiation-induced cell death in the mouse testis: relationship to apoptosis. Radiat. Res. 147, 457-467   DOI   ScienceOn
7 Kerr, J. F., A. H. Wyllie, and A. R. Currie. 1972. Apoptosis: a basic biological phenomenon with wide-ranging implications in tissue kinetics. Br. J. Cancer 26, 239-257   DOI   ScienceOn
8 Howell, S. J. and S. M. Shalet. 2005. Spermatogenesis after cancer treatment: damage and recovery. J. Natl. Cancer Inst. Monogr. 34, 12-17
9 Huckins, C. and E. F. Oakberg. 1978. Morphological and quantitative analysis of spermatogonia in mouse testes using whole mounted seminiferous tubules. II. The irradiated testes. Anat. Rec. 192, 529-542   DOI   ScienceOn
10 Kamiguchi, Y. and H. Tateno. 2002. Radiation- and chemical-induced structural chromosome aberrations in human spermatozoa. Mutat. Res. 504, 183-191   DOI   ScienceOn
11 Liu, G., P. Gong, H. Zhao, Z. Wang, S. Gong, and L. Cai. 2006. Effect of low-level radiation on the death of male germ cells. Radiat. Res. 165, 379-389   DOI   ScienceOn
12 Miura, M., I. Sasagawa, Y. Suzuki, T. Nakada, and J. Fujii. 2002. Apoptosis and expression of apoptosis-related genes in the mouse testis following heat exposure. Fertil. Steril. 77, 787-793   DOI   ScienceOn
13 Moon, C., C. W. Jeong, H. Kim, M. Ahn, S. Kim, and T. Shin. 2006. Expression of CD44 adhesion molecule in rat testis with ischemia/reperfusion injury. J. Vet. Med. Sci. 68, 761-764   DOI   ScienceOn
14 Eastman, A. 1993. Apoptosis: a product of programmed and unprogrammed cell death. Toxicol. Appl. Pharmacol. 121, 160-164   DOI   ScienceOn
15 Allan, D. J., G. C. Gobe, and B. V. Harmon. 1987. Cell death in spermatogenesis, pp. 229-258, In Potten, C. S. (ed.), Perspectives on Mammalian Cell Death, Oxford University Press, Oxford